GLT8D2 抗体 (AA 85-180) (HRP)
Our Local Distributor
北京 101111
Quick Overview for GLT8D2 抗体 (AA 85-180) (HRP) (ABIN1416178)
抗原
See all GLT8D2 抗体适用
宿主
克隆类型
标记
应用范围
-
-
抗原表位
- AA 85-180
-
交叉反应
- 人
-
预测反应
- Mouse,Rat,Dog,Cow,Horse,Rabbit
-
纯化方法
- Purified by Protein A.
-
免疫原
- KLH conjugated synthetic peptide derived from human GLT8D2
-
亚型
- IgG
-
-
anti-Glycosyltransferase 8 Domain Containing 2 (GLT8D2) (AA 25-349) antibody
GLT8D2 适用: 人 WB, ELISA 宿主: 兔 Polyclonal unconjugated
anti-Glycosyltransferase 8 Domain Containing 2 (GLT8D2) (C-Term) antibodyGLT8D2 适用: 人, 小鼠, 大鼠, 豚鼠, 兔, 猴 WB 宿主: 兔 Polyclonal unconjugated
anti-Glycosyltransferase 8 Domain Containing 2 (GLT8D2) (C-Term) antibodyGLT8D2 适用: 人, 小鼠, 大鼠 WB 宿主: 兔 Polyclonal unconjugated
anti-Glycosyltransferase 8 Domain Containing 2 (GLT8D2) (AA 14-42), (N-Term) antibodyGLT8D2 适用: 人 WB, FACS 宿主: 兔 Polyclonal RB24966 unconjugated
-
-
应用备注
-
WB 1:300-5000
IHC-P 1:200-400
IHC-F 1:100-500 -
限制
- 仅限研究用
-
-
-
状态
- Liquid
-
浓度
- 1 μg/μL
-
缓冲液
- Aqueous buffered solution containing 0.01M TBS ( pH 7.4) with 1 % BSA, 0.03 % Proclin300 and 50 % Glycerol.
-
储存液
- ProClin
-
注意事项
- This product contains ProClin: a POISONOUS AND HAZARDOUS SUBSTANCE, which should be handled by trained staff only.
-
注意事项
- Do NOT add Sodium Azide! Use of Sodium Azide will inhibit enzyme activity of horseradish peroxidase.
-
储存条件
- -20 °C
-
储存方法
- Store at -20°C. Aliquot into multiple vials to avoid repeated freeze-thaw cycles.
-
有效期
- 12 months
-
-
- GLT8D2 (Glycosyltransferase 8 Domain Containing 2 (GLT8D2))
-
别名
- GLT8D2
-
背景
-
Synonyms: GALA4A, GL8D2_HUMAN, GLT8D2, Glycosyltransferase 8 domain containing 2, Glycosyltransferase 8 domain-containing protein 2, Gycosyltransferase.
Background: GLT8D2 (glycosyltransferase 8 domain-containing protein 2), also known as GALA4A, is a 349 amino acid single-pass type II membrane protein. A member of the glycosyltransferase 8 family, GLT8D2 is encoded by a gene that maps to human chromosome 12q23.3. Encoding over 1,100 genes within 132 million base pairs, chromosome 12 makes up about 4.5 % of the human genome. A number of skeletal deformities are linked to chromosome 12, including hypochondrogenesis, achondrogenesis, Noonan syndrome, Kniest dysplasia and trisomy 12p. Chromosome 12 is also home to a homeobox gene cluster, which encodes crucial transcription factors for morphogenesis, as well as the natural killer complex gene cluster, which encodes C-type lectin proteins that mediate the NK cell response to MHC I interaction.
-
基因ID
- 83468
抗原
-
